Using our analytical strategy, we found a similar evolving nature in infiltrating immune cell components during tumor progression; that is, TIL subpopulations related to innate immunity, such as macrophage M0, macrophage M1, neutrophils, and resting dendritic cells, were enriched in the high-risk group, whereas TILs related to adaptive immunity, such as memory B cells, naive CD4 T cells, and gamma delta T cells (Tγδ), were enriched in the low-risk group. Here, CD4 is linked to neoplasm.